Stk16 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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31 records found for search term Stk16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156267900	CV2305706	single nucleotide variant	NM_001330213.2(STK16):c.77T>G (p.Leu26Arg)	not specified [RCV004167527]	uncertain significance	2	219246076	219246076	Human		name
407530121	CV3485493	single nucleotide variant	NM_001330213.2(STK16):c.95G>A (p.Ser32Asn)	not specified [RCV004681663]	uncertain significance	2	219246665	219246665	Human		name
598251470	CV3919670	single nucleotide variant	NM_001330213.2(STK16):c.55C>T (p.Arg19Cys)	not specified [RCV005277894]	uncertain significance	2	219246054	219246054	Human		name
156289039	CV2229856	single nucleotide variant	NM_001330213.2(STK16):c.236G>A (p.Arg79His)	not specified [RCV004105420]	uncertain significance	2	219246806	219246806	Human		name
156011015	CV2291097	single nucleotide variant	NM_001330213.2(STK16):c.115G>T (p.Gly39Trp)	not specified [RCV004151623]	uncertain significance	2	219246685	219246685	Human		name
401728189	CV2676000	single nucleotide variant	NM_001330213.2(STK16):c.266G>T (p.Gly89Val)	not specified [RCV004281990]	uncertain significance	2	219246836	219246836	Human		name
401749154	CV2713794	single nucleotide variant	NM_001330213.2(STK16):c.205C>T (p.His69Tyr)	not specified [RCV004321136]	uncertain significance	2	219246775	219246775	Human		name
401765126	CV2733500	single nucleotide variant	NM_001330213.2(STK16):c.235C>T (p.Arg79Cys)	not specified [RCV004330413]	uncertain significance	2	219246805	219246805	Human		name
405741465	CV3334455	single nucleotide variant	NM_001330213.2(STK16):c.191G>A (p.Arg64Gln)	not specified [RCV004465668]	uncertain significance	2	219246761	219246761	Human		name
405741458	CV3334456	single nucleotide variant	NM_001330213.2(STK16):c.229A>G (p.Ile77Val)	not specified [RCV004465669]	uncertain significance	2	219246799	219246799	Human		name
597747561	CV3614825	single nucleotide variant	NM_001330213.2(STK16):c.135C>G (p.Phe45Leu)	not specified [RCV004866088]	uncertain significance	2	219246705	219246705	Human		name
597747566	CV3614826	single nucleotide variant	NM_001330213.2(STK16):c.122A>G (p.His41Arg)	not specified [RCV004866089]	uncertain significance	2	219246692	219246692	Human		name
598207447	CV3919669	single nucleotide variant	NM_001330213.2(STK16):c.241G>A (p.Val81Met)	not specified [RCV005291285]	uncertain significance	2	219246811	219246811	Human		name
156253169	CV2192992	single nucleotide variant	NM_001330213.2(STK16):c.709A>G (p.Met237Val)	not specified [RCV004069545]	uncertain significance	2	219248244	219248244	Human		name
155971191	CV2237373	single nucleotide variant	NM_001330213.2(STK16):c.359T>C (p.Leu120Pro)	not specified [RCV004104562]	uncertain significance	2	219247165	219247165	Human		name
155923015	CV2340720	single nucleotide variant	NM_001330213.2(STK16):c.338T>A (p.Leu113Gln)	not specified [RCV004190390]	uncertain significance	2	219247144	219247144	Human		name
156005766	CV2401128	single nucleotide variant	NM_001330213.2(STK16):c.823G>A (p.Val275Met)	not specified [RCV004245693]	uncertain significance	2	219248464	219248464	Human		name
401740766	CV2680473	single nucleotide variant	NM_001330213.2(STK16):c.772A>G (p.Ser258Gly)	not specified [RCV004291116]	uncertain significance	2	219248307	219248307	Human		name
401862967	CV2755745	single nucleotide variant	NM_001330213.2(STK16):c.712G>C (p.Val238Leu)	not specified [RCV004342125]	uncertain significance	2	219248247	219248247	Human		name
401889241	CV2759740	single nucleotide variant	NM_001330213.2(STK16):c.596G>A (p.Arg199Gln)	not specified [RCV004342788]	uncertain significance	2	219247696	219247696	Human		name
401871050	CV2789001	single nucleotide variant	NM_001330213.2(STK16):c.788C>T (p.Ser263Leu)	not specified [RCV004363313]	uncertain significance	2	219248429	219248429	Human		name
405741451	CV3334457	single nucleotide variant	NM_001330213.2(STK16):c.379T>C (p.Trp127Arg)	not specified [RCV004465670]	uncertain significance	2	219247185	219247185	Human		name
405741237	CV3334458	single nucleotide variant	NM_001330213.2(STK16):c.467T>C (p.Leu156Pro)	not specified [RCV004465671]	uncertain significance	2	219247441	219247441	Human		name
405741045	CV3334459	single nucleotide variant	NM_001330213.2(STK16):c.577C>T (p.Arg193Trp)	not specified [RCV004465672]	uncertain significance	2	219247677	219247677	Human		name
405740864	CV3334460	single nucleotide variant	NM_001330213.2(STK16):c.643C>T (p.Arg215Trp)	not specified [RCV004465673]	uncertain significance	2	219247743	219247743	Human		name
405740744	CV3334461	single nucleotide variant	NM_001330213.2(STK16):c.682A>G (p.Met228Val)	not specified [RCV004465674]	uncertain significance	2	219248217	219248217	Human		name
597747571	CV3614828	single nucleotide variant	NM_001330213.2(STK16):c.800A>T (p.Gln267Leu)	not specified [RCV004866090]	uncertain significance	2	219248441	219248441	Human		name
598207425	CV3919665	single nucleotide variant	NM_001330213.2(STK16):c.314C>T (p.Thr105Met)	not specified [RCV005291282]	uncertain significance	2	219247120	219247120	Human		name
598207434	CV3919666	single nucleotide variant	NM_001330213.2(STK16):c.892C>T (p.Pro298Ser)	not specified [RCV005291283]	uncertain significance	2	219248533	219248533	Human		name
598251465	CV3919667	single nucleotide variant	NM_001330213.2(STK16):c.621G>C (p.Gln207His)	not specified [RCV005277893]	uncertain significance	2	219247721	219247721	Human		name
598207441	CV3919668	single nucleotide variant	NM_001330213.2(STK16):c.902A>G (p.His301Arg)	not specified [RCV005291284]	uncertain significance	2	219248543	219248543	Human		name

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